Refined Mapping of a Gene Responsible for Fukuyama-Type Congenital Muscular Dystrophy: Evidence for Strong Linkage Disequilibrium

Fukuyama-type congenital muscular dystrophy (FCMD), the second most common form of childhood muscular dystrophy in Japan, is an autosomal recessive severe muscular dystrophy associated with an anomaly of the brain. After our initial mapping of the FCMD locus to chromosome 9q31-33, we further defined...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Toda, Tatsushi, Ikegawa, Shiro, Okui, Keiko, Kondo, Eri, Saito, Kayoko, Fukuyama, Yukio, Yoshioka, Mieko, Kumagai, Toshiyuki, Suzumori, Kaoru, Kanazawa, Ichiro, Nakamura, Yusuke
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1994
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Original Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918318/
https://ncbi.nlm.nih.gov/pubmed/7977357
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